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Stannane, triphenyl(3,3,3-trifluoro-1-propynyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

503311-60-2

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503311-60-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 503311-60-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,3,3,1 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 503311-60:
(8*5)+(7*0)+(6*3)+(5*3)+(4*1)+(3*1)+(2*6)+(1*0)=92
92 % 10 = 2
So 503311-60-2 is a valid CAS Registry Number.

503311-60-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name triphenyl(3,3,3-trifluoroprop-1-ynyl)stannane

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:503311-60-2 SDS

503311-60-2Relevant academic research and scientific papers

Amide derivatives as ion-channel ligands and pharmaceutical compositions and methods of using the same

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Page/Page column 32, (2008/06/13)

Compounds are disclosed that have a formula represented by the following: The compounds may be prepared as pharmaceutical compositions, and may be used for the prevention and treatment of a variety of conditions in mammals including humans, including by way of non-limiting example, pain, inflammation, traumatic injury, and others.

Preparation and Functionalization of a Range of Main-Group Trifluoropropynyl Organometallic Compounds: The Application of Metalloid-Directed Carbolithiation to the Selective Synthesis of Novel Fluorocarbon Fragments

Brisdon, Alan K.,Crossley, Ian R.,Pritchard, Robin G.,Sadiq, Ghazala,Warren, John E.

, p. 5534 - 5542 (2008/10/09)

The reaction of 1,1,1,3,3-pentafluoropropane (CF3CH 2CF2H, HFC-245fa) with 3 equiv of n-butyllithium at -10 °C leads to the generation of trifluoropropynyllithium in excellent yields. This reagent reacts readily with a range of group 14 electrophiles R 4-n-EXn (R = Ph, Et; E = C, Si, Ge, Sn, Pb; X = Cl, Br) to yield the organometalloid trifluoropropynyl compounds R 4-nE(C≡CCF3)n. Three of these compounds, Ph3EC≡CCF3 (E = C, Si, Ge), have been crystallographically characterized, representing the first such study of these materials. The silane Ph3SiC≡CCF3 has been derivatized by reaction with LiAlH4 and a range of organolithium reagents (RLi, R = n-Bu, Ph, t-Bu) to afford a new series of β-CF 3-substituted vinylsilanes of the type Ph3SiCH=C(CF 3)R, with predominantly E geometry at the double bond. In the cases R = n-Bu, t-Bu, and Ph, these materials have been crystallographically characterized. Additionally, a remarkably facile cyclization pathway for Ph 3Si≡CCF3, initiated by t-BuLi, that yields the respective gem-difluorocyclopropene has been explored and is described in detail, along with its extension to a number of other systems.

Hydrofluorocarbon 245fa: A versatile new synthon in alkyne chemistry

Brisdon, Alan K.,Crossley, Ian R.

, p. 2420 - 2421 (2007/10/03)

The CFC replacement 1,1,1,3,3-pentafluoropropane (HFC 245fa) has been established as a convenient source of trifluoropropynyllithium under mild conditions; a range of novel and known trifluoropropynyl-containing systems has been prepared in a one-pot procedure.

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